Canonical Allele Identifier: CA1975539234

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945515529

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614473_57614474insGA , CM000673.2:g.57614473_57614474insGA	GRCh38
NC_000011.9:g.57381946_57381947insGA , CM000673.1:g.57381946_57381947insGA	GRCh37
NC_000011.8:g.57138522_57138523insGA	NCBI36
NG_009625.1:g.21920_21921insGA , LRG_105:g.21920_21921insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1395_1396insGA MANE Select	ENSP00000278407.4:p.Arg466AspfsTer?
ENST00000528996.2:c.*292_*293insGA	ENSP00000431226.2:n.*292_*293insGA
ENST00000531605.2:c.*1171_*1172insGA	ENSP00000503752.1:n.*1171_*1172insGA
ENST00000619430.2:c.1191_1192insGA	ENSP00000478572.2:p.Arg398AspfsTer?
ENST00000676670.1:c.1395_1396insGA	ENSP00000504807.1:p.Arg466AspfsTer?
ENST00000676741.1:n.2477_2478insGA
ENST00000677624.1:c.*815_*816insGA	ENSP00000503979.1:n.*815_*816insGA
ENST00000677625.1:c.1341_1342insGA	ENSP00000502857.1:p.Arg448AspfsTer?
ENST00000677856.1:n.1648_1649insGA
ENST00000677915.1:c.*292_*293insGA	ENSP00000503118.1:n.*292_*293insGA
ENST00000678533.1:c.*949_*950insGA	ENSP00000503873.1:n.*949_*950insGA
ENST00000678592.1:c.*335_*336insGA	ENSP00000504424.1:n.*335_*336insGA
ENST00000278407.8:c.1395_1396insGA	ENSP00000278407.4:p.Arg466AspfsTer?
ENST00000340687.10:c.1284_1285insGA	ENSP00000341861.6:p.Arg429AspfsTer?
ENST00000378323.8:c.1410_1411insGA	ENSP00000367574.4:p.Arg471AspfsTer?
ENST00000378324.6:c.1239_1240insGA	ENSP00000367575.2:p.Arg414AspfsTer?
ENST00000403558.1:c.1524_1525insGA	ENSP00000384420.1:p.Arg509AspfsTer?
ENST00000528996.1:c.596_597insGA	ENSP00000431226.1:n.596_597insGA
ENST00000530113.1:n.852_853insGA
ENST00000531133.5:c.896_897insGA	ENSP00000435431.1:n.896_897insGA
ENST00000531797.5:c.*420_*421insGA	ENSP00000432554.1:n.*420_*421insGA
ENST00000619430.1:c.526_527insGA	ENSP00000478572.1:n.526_527insGA
NM_000062.2:c.1395_1396insGA , LRG_105t1:c.1395_1396insGA	NP_000053.2:p.Arg466AspfsTer?
NM_001032295.1:c.1395_1396insGA	NP_001027466.1:p.Arg466AspfsTer?
NM_000062.3:c.1395_1396insGA MANE Select	NP_000053.2:p.Arg466AspfsTer?
NM_001032295.2:c.1395_1396insGA	NP_001027466.1:p.Arg466AspfsTer?